1998
DOI: 10.1016/s0022-2143(98)90047-6
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Are phospholipase A2 and nitric oxide involved in the alterations in peritoneal transport during CAPD peritonitis?

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Cited by 39 publications
(22 citation statements)
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“…28,29 Vasoactive substances released during the inflammation reaction, particularly NO, play a role in these changes. 30 Indeed, inhibition of NOS with N G -nitro-L-arginine methyl ester improve UF and reverse permeability changes in rat and mouse models of acute peritonitis. 8,31 The three NOS isoforms-neuronal NOS (nNOS, NOS1), inducible NOS (iNOS, NOS2), and eNOS (NOS3)-are differentially expressed in the peritoneal membrane.…”
Section: Acute Peritonitis: Role Of Nos Isoformsmentioning
confidence: 99%
“…28,29 Vasoactive substances released during the inflammation reaction, particularly NO, play a role in these changes. 30 Indeed, inhibition of NOS with N G -nitro-L-arginine methyl ester improve UF and reverse permeability changes in rat and mouse models of acute peritonitis. 8,31 The three NOS isoforms-neuronal NOS (nNOS, NOS1), inducible NOS (iNOS, NOS2), and eNOS (NOS3)-are differentially expressed in the peritoneal membrane.…”
Section: Acute Peritonitis: Role Of Nos Isoformsmentioning
confidence: 99%
“…Acute peritonitis is associated with increased peritoneal transport rates of low molecular weight solutes and serum proteins [22,23]. This points to an inflammationinduced increase in the effective peritoneal surface area caused by a larger number of perfused microvessels and vasodilation.…”
Section: Peritoneal Transport and Inflammatory Mediators During Peritmentioning
confidence: 99%
“…This points to an inflammationinduced increase in the effective peritoneal surface area caused by a larger number of perfused microvessels and vasodilation. This is supported by the higher peritoneal blood flow during peritonitis than after recovery from the infection [23]. In addition a reduced size selectivity is present in the early phase [5], leading to a decrease in the peritoneal restriction coefficient to macromolecules [24].…”
Section: Peritoneal Transport and Inflammatory Mediators During Peritmentioning
confidence: 99%
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